Allele Registry

Canonical Allele Identifier: PA2825202867

Gene: ELN HGNC NCBI

ClinVar RCV:

RCV001327086

ClinVar Variation:

1026613

HGVS (amino-acid)	Matching Registered Transcripts
NP_000492.2:p.Gly620Arg	CA367889574 NM_000501.4:c.1858G>C CA367889575 NM_000501.4:c.1858G>A